Department of Clinical Neurosciences, University of Cambridge Metabolic Research Laboratories, NIHR Biomedical Research Centre, Institute of Metabolic Science, University of Cambridge, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
Department of Clinical Neurosciences, University of Cambridge Metabolic Research Laboratories, NIHR Biomedical Research Centre, Institute of Metabolic Science, University of Cambridge, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
FEBS Lett. 2014 Aug 1;588(15):2477-83. doi: 10.1016/j.febslet.2014.06.005. Epub 2014 Jun 6.
Circadian rhythms enable organisms to co-ordinate biological processes with the predictable 24 h cycle of day and night. Given that molecular clocks that coordinate such biological timing have evolved in almost all organisms, it is clear that being synchronous with the external environment confers competitive advantage. Conversely, it is apparent that being out of phase is detrimental, resulting in a number of clinical conditions, many of which are linked to metabolic dysfunction. The canonical clockwork involves a core set of genes that negatively regulate themselves through a so-called transcription translation feedback loop. However, recent studies describing evolutionarily conserved oscillations in redox reactions link circadian rhythms to metabolic processes, and in particular, redox pathways. In this review we describe the evidence for the interaction between transcriptional loops, redox and metabolism in mammals and suggest the clock may be potential target for the treatment of disease.
昼夜节律使生物体能够将生物过程与白天和黑夜的可预测 24 小时周期协调一致。鉴于协调这种生物定时的分子钟几乎在所有生物体中都有进化,很明显与外部环境同步会带来竞争优势。相反,不同步显然是有害的,导致许多临床病症,其中许多与代谢功能障碍有关。典型的时钟装置涉及一组核心基因,它们通过所谓的转录翻译反馈环自我负调控。然而,最近描述氧化还原反应中进化上保守的振荡的研究将昼夜节律与代谢过程联系起来,特别是与氧化还原途径联系起来。在这篇综述中,我们描述了转录环、氧化还原和哺乳动物代谢之间相互作用的证据,并提出时钟可能是治疗疾病的潜在靶点。